Canonical Allele Identifier: CA2520754033
Gene: MBL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52771495del , CM000672.2:g.52771495del GRCh38
NC_000010.10:g.54531255del , CM000672.1:g.54531255del GRCh37
NC_000010.9:g.54201261del NCBI36
NG_008196.1:g.5206del , LRG_154:g.5206del

Transcript Alleles

HGVS Amino-acid change
ENST00000674931.1:c.141del MANE Select ENSP00000502789.1:p.Gly48AlafsTer?
ENST00000675947.1:c.141del ENSP00000502615.1:p.Gly48AlafsTer?
ENST00000373968.3:c.141del ENSP00000363079.3:p.Gly48AlafsTer?
NM_000242.2:c.141del , LRG_154t1:c.141del NP_000233.1:p.Gly48AlafsTer?
XM_006717861.2:c.141del XP_006717924.1:p.Gly48AlafsTer?
XM_011539816.1:c.141del XP_011538118.1:p.Gly48AlafsTer?
XM_006717861.4:c.141del XP_006717924.1:p.Gly48AlafsTer?
XM_011539816.3:c.141del XP_011538118.1:p.Gly48AlafsTer?
NM_000242.3:c.141del NP_000233.1:p.Gly48AlafsTer?
NM_001378373.1:c.141del MANE Select NP_001365302.1:p.Gly48AlafsTer?
NM_001378374.1:c.141del NP_001365303.1:p.Gly48AlafsTer?